US9498773B2ActiveUtilityA1
Catalyst system for olefin oligomerization, and method for olefin oligomerization using the same
Est. expiryNov 18, 2033(~7.4 yrs left)· nominal 20-yr term from priority
B01J 2231/20C07C 2/36C07C 2/32C07F 9/46C07C 2531/18B01J 31/2213C07C 2531/22B01J 31/186C07F 9/535C07C 2531/24B01J 31/2414C07C 2531/14C07F 9/5018B01J 31/00C08F 4/42B01J 31/34B01J 31/189B01J 31/143C07F 9/5027B01J 2531/62C07C 11/107C07C 11/02
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Claims
Abstract
The present invention relates to a compound represented by Chemical Formula 1, a catalyst system for olefin oligomerization comprising the same, and a method of olefin oligomerization using the same.
Claims
exact text as granted — not AI-modifiedThe invention claimed is:
1. A catalyst system for olefin oligomerization, comprising a compound represented by the following Chemical Formula 1, a source of a transition metal, and a cocatalyst:
wherein, in Chemical Formula 1,
A is represented by the following Chemical Formula 2,
X is a C 1-20 alkylene or a C 6-14 arylene,
R 1 to R 4 are independently a C 1-20 alkyl, a C 2-20 alkenyl, a C 6-14 aryl, a C 6-14 aryl substituted with a C 1-4 alkyl, a C 1-4 alkyl substituted with a C 6-14 aryl, or a C 6-14 aryl substituted with a C 1-4 alkoxy,
R 5 to R 14 are independently hydrogen, a C 1-20 alkyl, a C 2-20 alkenyl, a C 6-14 aryl, a C 6-14 aryl substituted with a C 1-4 alkyl, a C 1-4 alkyl substituted with a C 6-14 aryl, or a C 6-14 aryl substituted with a C 1-4 alkoxy.
2. The catalyst system according to claim 1 , wherein X is methylene or phenylene.
3. The catalyst system according to claim 1 , wherein R 1 to R 4 are identical to each other.
4. The catalyst system according to claim 1 , wherein R 1 to R 4 are phenyl.
5. The catalyst system according to claim 1 , wherein R 5 and R 6 are hydrogen.
6. The catalyst system according to claim 1 , wherein R 7 and R 8 are identical to each other, and are hydrogen or methyl.
7. The catalyst system according to claim 1 , wherein R 9 is hydrogen or iso-propyl.
8. The catalyst system according to claim 7 , wherein R 10 is hydrogen.
9. The catalyst system according to claim 1 , wherein R 11 to R 13 are hydrogen.
10. The catalyst system according to claim 1 , wherein R 14 is hydrogen or methyl.
11. The catalyst system according to claim 1 , wherein the compound is selected from the group consisting of the following compounds:
12. The catalyst system according to claim 1 , wherein the source of a transition metal is at least one selected from the group consisting of chromium(III)acetylacetonate, tris(tetrahydrofuran)chromium trichloride, chromium(III)-2-ethylhexanoate, chromium(III)tris(2,2,6,6-tetramethyl-3,5-heptanedionate), chromium(III)benzoylacetonate, chromium(III)hexafluoro-2,4-pentanedionate, and chromium(III)acetate hydroxide.
13. The catalyst system according to claim 1 , wherein the cocatalyst is at least one selected from the group consisting of the compounds represented by the following Chemical Formulae 3 to 5:
—[Al(R 15 )—O] c — [Chemical Formula 3]
in Chemical Formula 3,
R 15 's are independently a halogen, a C 1-20 alkyl, or a C 1-20 haloalkyl, and
c is an integer equal to or greater than 2,
D(R 16 ) 3 [Chemical Formula 4]
in Chemical Formula 4,
D is aluminum or boron, and
R 16 is a C 1-20 alkyl or a C 1-20 haloalkyl,
[L-H] + [Q(E) 4 ] − [Chemical Formula 5]
in Chemical Formula 5,
L is a neutral Lewis base,
[L-H ] + is a Bronsted acid,
Q is B or Al, and
E's are independently a C 6-20 aryl or a C 1-20 alkyl, and are unsubstituted or substituted with at least one substituent selected from the group consisting of a halogen, a C 1-20 alkyl, a C 1-20 alkoxy, and a phenoxy.
14. A method for olefin oligomerization, comprising the step of oligomerizing olefins in the presence of the catalyst system for olefin oligomerization according to claim 1 .Cited by (0)
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